Clinical Research Implementation Office (CRIO)

Mission

The CRIO team will ensure agile, responsive, evidence-based tools and guidance for clinical translational research and clinical trial implementation across the research lifecycle from concept through publication, 91PORN-wide. 

Goal

CRIO chart

Our Team

With a combined 30+ years of NIH RO1/UG3-UH3, multi-site CPRIT, DoD and sponsored clinical research experience, our team is here to help principal investigators and study teams across all schools, departments and divisions.

Stephanie D. Rowan, Ph.D., M.N., R.N. Picture

Stephanie D. Rowan, Ph.D., M.N., R.N.
Director, CRIO

 

 

Karen Nijland, B. Pharm Picture

Karen Nijland, B. Pharm
Research Compliance Coordinator – Senior
ClinicalTrials.gov Institutional Administrator
FDA Submissions Program Manager

 

Our Resources   

  • Study Start-up Checklists  
  • Study Timeline Templates with milestones
  • Recruitment & Retention Plans & Guidance 
  • Investigator Initiated Study Protocol Templates
  • Data Collection Case Report Form (CRFs) Templates & Guidance
  • Regulatory File guidance and Templates, including Complion e-Regulatory System 
  • Clinical Trials.gov Registration & Reporting assistance
  • Team Science, Training, Collaboration & Resources 
  • FDA IND/IDE Registration & Reporting assistance 
  • Study Team Onboarding Templates & Guidance 
  • Training for Study Start Up Acceleration

Contact Us

Please contact CRIO@uthscsa.edu if you have any questions.

Complete a for a 30-minute scheduled consultation with our CRIO staff.

91PORN faculty and staff can click here to learn more.